A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26133



Internal ID15832636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97554323..97557757hg38UCSC Ensembl
Outerchr15:97553913..97559040hg38UCSC Ensembl
Innerchr15:98097553..98100987hg19UCSC Ensembl
Outerchr15:98097143..98102270hg19UCSC Ensembl
Innerchr15:95898557..95901991hg18UCSC Ensembl
Outerchr15:95898147..95903274hg18UCSC Ensembl
Innerchr15:95898557..95901991hg17UCSC Ensembl
Outerchr15:95898147..95903274hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385128
hg195128
hg185128
hg175128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9303
Supporting Variants
SamplesNA18502
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv26133
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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